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GTR Home > Laboratories > Bioscientia GmbH

Bioscientia GmbH

GTR Lab ID: 256837, Last updated:2019-09-24
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Personnel

Conditions and tests

  • 11p partial monosomy syndrome1 test
  • 3M syndrome 11 test
  • ABCD syndrome1 test
  • Achondroplasia1 test
  • Acrocephalosyndactyly type I1 test
  • Acromesomelic dysplasia 1, Maroteaux type1 test
  • Acromesomelic dysplasia 2C, Hunter-Thompson type1 test
  • Adrenoleukodystrophy2 tests
  • Alagille syndrome due to a JAG1 point mutation1 test
  • Alagille syndrome due to a NOTCH2 point mutation1 test
  • Alpha-1-antitrypsin deficiency1 test
  • Alport syndrome1 test
  • Andersen Tawil syndrome1 test
  • Angelman syndrome1 test
  • Angiokeratoma corporis diffusum1 test
  • Aniridia 11 test
  • Anonychia1 test
  • Anophthalmia-microphthalmia syndrome1 test
  • Arthrogryposis, renal dysfunction, and cholestasis 11 test
  • Atypical hemolytic-uremic syndrome with C3 anomaly1 test
  • Atypical hemolytic-uremic syndrome with I factor anomaly1 test
  • Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly1 test
  • Autosomal dominant Alport syndrome2 tests
  • Autosomal dominant hypophosphatemic rickets1 test
  • Autosomal dominant nonsyndromic hearing loss 11 test
  • Autosomal dominant nonsyndromic hearing loss 101 test
  • Autosomal dominant nonsyndromic hearing loss 111 test
  • Autosomal dominant nonsyndromic hearing loss 121 test
  • Autosomal dominant nonsyndromic hearing loss 131 test
  • Autosomal dominant nonsyndromic hearing loss 151 test
  • Autosomal dominant nonsyndromic hearing loss 171 test
  • Autosomal dominant nonsyndromic hearing loss 201 test
  • Autosomal dominant nonsyndromic hearing loss 221 test
  • Autosomal dominant nonsyndromic hearing loss 251 test
  • Autosomal dominant nonsyndromic hearing loss 281 test
  • Autosomal dominant nonsyndromic hearing loss 2A1 test
  • Autosomal dominant nonsyndromic hearing loss 2B1 test
  • Autosomal dominant nonsyndromic hearing loss 361 test
  • Autosomal dominant nonsyndromic hearing loss 3A1 test
  • Autosomal dominant nonsyndromic hearing loss 3B1 test
  • Autosomal dominant nonsyndromic hearing loss 441 test
  • Autosomal dominant nonsyndromic hearing loss 481 test
  • Autosomal dominant nonsyndromic hearing loss 4A1 test
  • Autosomal dominant nonsyndromic hearing loss 51 test
  • Autosomal dominant nonsyndromic hearing loss 61 test
  • Autosomal dominant nonsyndromic hearing loss 91 test
  • Autosomal recessive Alport syndrome2 tests
  • Autosomal recessive nonsyndromic hearing loss 121 test
  • Autosomal recessive nonsyndromic hearing loss 18A1 test
  • Autosomal recessive nonsyndromic hearing loss 1A2 tests
  • Autosomal recessive nonsyndromic hearing loss 21 test
  • Autosomal recessive nonsyndromic hearing loss 211 test
  • Autosomal recessive nonsyndromic hearing loss 221 test
  • Autosomal recessive nonsyndromic hearing loss 231 test
  • Autosomal recessive nonsyndromic hearing loss 241 test
  • Autosomal recessive nonsyndromic hearing loss 281 test
  • Autosomal recessive nonsyndromic hearing loss 291 test
  • Autosomal recessive nonsyndromic hearing loss 31 test
  • Autosomal recessive nonsyndromic hearing loss 301 test
  • Autosomal recessive nonsyndromic hearing loss 311 test
  • Autosomal recessive nonsyndromic hearing loss 351 test
  • Autosomal recessive nonsyndromic hearing loss 361 test
  • Autosomal recessive nonsyndromic hearing loss 371 test
  • Autosomal recessive nonsyndromic hearing loss 391 test
  • Autosomal recessive nonsyndromic hearing loss 491 test
  • Autosomal recessive nonsyndromic hearing loss 591 test
  • Autosomal recessive nonsyndromic hearing loss 61 test
  • Autosomal recessive nonsyndromic hearing loss 631 test
  • Autosomal recessive nonsyndromic hearing loss 671 test
  • Autosomal recessive nonsyndromic hearing loss 71 test
  • Autosomal recessive nonsyndromic hearing loss 771 test
  • Autosomal recessive nonsyndromic hearing loss 91 test
  • Autosomal recessive polycystic kidney disease1 test
  • Autosomal recessive Robinow syndrome1 test
  • Baraitser-winter syndrome 21 test
  • Bardet-Biedl syndrome 11 test
  • Bardet-Biedl syndrome 101 test
  • Bardet-Biedl syndrome 111 test
  • Bardet-Biedl syndrome 121 test
  • Bardet-Biedl syndrome 131 test
  • Bardet-Biedl syndrome 141 test
  • Bardet-Biedl syndrome 151 test
  • Bardet-Biedl syndrome 21 test
  • Bardet-Biedl syndrome 31 test
  • Bardet-Biedl syndrome 41 test
  • Bardet-Biedl syndrome 51 test
  • Bardet-Biedl syndrome 61 test
  • Bardet-Biedl syndrome 71 test
  • Bardet-Biedl syndrome 81 test
  • Bardet-Biedl syndrome 91 test
  • Bartter disease type 11 test
  • Bartter disease type 21 test
  • Bartter disease type 31 test
  • Bartter disease type 4a1 test
  • Beckwith-Wiedemann syndrome1 test
  • Biotin-responsive basal ganglia disease1 test
  • Borjeson-Forssman-Lehmann syndrome1 test
  • Brachydactyly type C1 test
  • Branchiootic syndrome 31 test
  • Branchiootorenal syndrome 11 test
  • Branchiootorenal syndrome 21 test
  • Breast-ovarian cancer, familial, susceptibility to, 11 test
  • Breast-ovarian cancer, familial, susceptibility to, 21 test
  • Brugada syndrome 11 test
  • Camptomelic dysplasia1 test
  • Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 11 test
  • Ceroid lipofuscinosis, neuronal, 6A1 test
  • CFHR5-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II1 test
  • Charcot-Marie-Tooth disease dominant intermediate B1 test
  • Charcot-Marie-Tooth disease type 1B1 test
  • Charcot-Marie-Tooth disease type 1D1 test
  • Charcot-Marie-Tooth disease type 1E1 test
  • Charcot-Marie-Tooth disease type 2A21 test
  • Charcot-Marie-Tooth disease type 4A1 test
  • Charcot-Marie-Tooth disease type 4E1 test
  • Charcot-Marie-Tooth disease type 4F1 test
  • Charcot-Marie-Tooth disease X-linked dominant 11 test
  • Charcot-Marie-Tooth Neuropathy Type 2H/2K1 test
  • CHARGE association1 test
  • Chronic infantile neurological, cutaneous and articular syndrome1 test
  • Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency1 test
  • Cleidocranial dysostosis1 test
  • Cockayne syndrome type 11 test
  • Cockayne syndrome type 21 test
  • Cold-induced sweating syndrome 11 test
  • Congenital secretory diarrhea, chloride type1 test
  • Congenital stromal corneal dystrophy1 test
  • Cornelia de Lange syndrome 11 test
  • Crigler-Najjar syndrome1 test
  • Cystic fibrosis1 test
  • Dent disease type 11 test
  • Dent disease type 21 test
  • Desbuquois dysplasia 11 test
  • DFNA 3 Nonsyndromic Hearing Loss and Deafness1 test
  • DFNB 8/10 Nonsyndromic Hearing Loss and Deafness1 test
  • Diabetes insipidus, nephrogenic, autosomal2 tests
  • Diabetes insipidus, nephrogenic, X-linked1 test
  • Dihydropyrimidine dehydrogenase deficiency1 test
  • Dilated cardiomyopathy 1E1 test
  • Dilated cardiomyopathy 3B1 test
  • Disorder of cardiovascular system3 tests
  • Early-onset generalized limb-onset dystonia1 test
  • Ehlers-Danlos syndrome type 7A1 test
  • Ehlers-Danlos syndrome type 7B1 test
  • Ehlers-Danlos syndrome, kyphoscoliotic type 11 test
  • Ehlers-Danlos syndrome, type 31 test
  • Ellis-van Creveld syndrome2 tests
  • Familial dysautonomia1 test
  • Familial hypocalciuric hypercalcemia 11 test
  • Familial hypokalemia-hypomagnesemia1 test
  • Familial juvenile hyperuricemic nephropathy type 11 test
  • Familial Mediterranean fever1 test
  • Familial X-linked hypophosphatemic vitamin D refractory rickets1 test
  • Feingold syndrome type 11 test
  • Focal segmental glomerulosclerosis 11 test
  • Focal segmental glomerulosclerosis 21 test
  • Focal segmental glomerulosclerosis 31 test
  • Focal segmental glomerulosclerosis 51 test
  • Fragile X syndrome1 test
  • G6PD deficiency1 test
  • Gilbert syndrome1 test
  • Glucocorticoid deficiency 11 test
  • Glucocorticoid deficiency 21 test
  • Glucocorticoid-remediable aldosteronism1 test
  • Grebe syndrome1 test
  • Greig cephalopolysyndactyly syndrome1 test
  • GTP cyclohydrolase I deficiency1 test
  • Hb SS disease1 test
  • Hemochromatosis type 11 test
  • Hemolytic uremic syndrome, atypical, susceptibility to, 11 test
  • Hereditary fructosuria1 test
  • Hereditary insensitivity to pain with anhidrosis1 test
  • Hereditary pancreatitis2 tests
  • Hereditary xanthinuria type 11 test
  • Holt-Oram syndrome1 test
  • Hypercholesterolemia, autosomal dominant, 31 test
  • Hypercholesterolemia, autosomal dominant, type B1 test
  • Hypercholesterolemia, familial, 11 test
  • Hypercholesterolemia, familial, 41 test
  • Hyperimmunoglobulin D with periodic fever1 test
  • Hyperinsulinemic hypoglycemia, familial, 11 test
  • Hyperinsulinism-hyperammonemia syndrome1 test
  • Hypertrophic cardiomyopathy 11 test
  • Hypertrophic cardiomyopathy 41 test
  • Hypertrophic osteoarthropathy, primary, autosomal recessive, 11 test
  • Hypochondroplasia1 test
  • Hypogonadotropic hypogonadism 1 with or without anosmia1 test
  • Hypogonadotropic hypogonadism 2 with or without anosmia1 test
  • Hypogonadotropic hypogonadism 3 with or without anosmia1 test
  • Hypoparathyroidism, deafness, renal disease syndrome1 test
  • Hypophosphatemic rickets, X-linked recessive1 test
  • Infantile cortical hyperostosis1 test
  • Inflammatory bowel disease 11 test
  • Insulin-dependent diabetes mellitus secretory diarrhea syndrome1 test
  • Joubert syndrome 11 test
  • Joubert syndrome 101 test
  • Joubert syndrome 131 test
  • Joubert syndrome 141 test
  • Joubert syndrome 21 test
  • Joubert syndrome 31 test
  • Joubert syndrome 51 test
  • Joubert syndrome 61 test
  • Joubert syndrome 71 test
  • Joubert syndrome 81 test
  • Joubert syndrome 91 test
  • Joubert syndrome with renal defect1 test
  • Junctional epidermolysis bullosa gravis of Herlitz2 tests
  • Kartagener syndrome1 test
  • Langer mesomelic dysplasia syndrome1 test
  • Leber congenital amaurosis 11 test
  • Leber congenital amaurosis 101 test
  • Leber congenital amaurosis 111 test
  • Leber congenital amaurosis 121 test
  • Leber congenital amaurosis 132 tests
  • Leber congenital amaurosis 141 test
  • Leber congenital amaurosis 21 test
  • Leber congenital amaurosis 31 test
  • Leber congenital amaurosis 41 test
  • Leber congenital amaurosis 51 test
  • Leber congenital amaurosis 61 test
  • Leber congenital amaurosis 71 test
  • Leber congenital amaurosis 81 test
  • LEOPARD syndrome 11 test
  • Leri-Weill dyschondrosteosis1 test
  • Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss1 test
  • Maturity-onset diabetes of the young type 21 test
  • Meckel syndrome, type 11 test
  • Meckel syndrome, type 111 test
  • Meckel syndrome, type 21 test
  • Meckel syndrome, type 31 test
  • Meckel syndrome, type 41 test
  • Meckel syndrome, type 51 test
  • Meckel syndrome, type 61 test
  • Melnick-Needles syndrome1 test
  • Metaphyseal chondrodysplasia, Schmid type1 test
  • Muenke syndrome1 test
  • Multiple endocrine neoplasia, type 21 test
  • Nail-patella syndrome1 test
  • Neonatal diabetes mellitus with congenital hypothyroidism1 test
  • Nephronophthisis 121 test
  • Nesidioblastosis1 test
  • Neurofibromatosis, type 11 test
  • Neurohypophyseal diabetes insipidus1 test
  • Neuronal ceroid lipofuscinosis 72 tests
  • Neuronal ceroid lipofuscinosis 81 test
  • Neuronopathy, distal hereditary motor, type 5A1 test
  • Non-acquired combined pituitary hormone deficiency with spine abnormalities1 test
  • Nonpersistence of intestinal lactase1 test
  • Noonan syndrome 11 test
  • Noonan syndrome 41 test
  • Obesity1 test
  • Obesity due to leptin receptor gene deficiency1 test
  • Obesity due to pro-opiomelanocortin deficiency1 test
  • Osteogenesis imperfecta1 test
  • Pendred syndrome1 test
  • Pfeiffer syndrome1 test
  • Pigmentary pallidal degeneration1 test
  • Pituitary hormone deficiency, combined, 21 test
  • Polycystic kidney disease 21 test
  • Polycystic kidney disease, adult type1 test
  • Prader-Willi syndrome1 test
  • Primary ciliary dyskinesia 31 test
  • Progressive familial intrahepatic cholestasis type 11 test
  • Progressive familial intrahepatic cholestasis type 21 test
  • Progressive familial intrahepatic cholestasis type 31 test
  • Qualitative or quantitative defects of dystrophin1 test
  • Retinitis pigmentosa 11 test
  • Retinitis pigmentosa 101 test
  • Retinitis pigmentosa 111 test
  • Retinitis pigmentosa 121 test
  • Retinitis pigmentosa 131 test
  • Retinitis pigmentosa 141 test
  • Retinitis pigmentosa 171 test
  • Retinitis pigmentosa 181 test
  • Retinitis pigmentosa 191 test
  • Retinitis pigmentosa 201 test
  • Retinitis pigmentosa 251 test
  • Retinitis pigmentosa 271 test
  • Retinitis pigmentosa 301 test
  • Retinitis pigmentosa 311 test
  • Retinitis pigmentosa 331 test
  • Retinitis pigmentosa 351 test
  • Retinitis pigmentosa 371 test
  • Retinitis pigmentosa 381 test
  • Retinitis pigmentosa 41 test
  • Retinitis pigmentosa 401 test
  • Retinitis pigmentosa 411 test
  • Retinitis pigmentosa 421 test
  • Retinitis pigmentosa 431 test
  • Retinitis pigmentosa 441 test
  • Retinitis pigmentosa 451 test
  • Retinitis pigmentosa 461 test
  • Retinitis pigmentosa 471 test
  • Retinitis pigmentosa 481 test
  • Retinitis pigmentosa 491 test
  • Retinitis pigmentosa 501 test
  • Retinitis pigmentosa 511 test
  • Retinitis pigmentosa 541 test
  • Retinitis pigmentosa 71 test
  • Retinitis pigmentosa 91 test
  • Severe myoclonic epilepsy in infancy1 test
  • Short-rib thoracic dysplasia 6 with or without polydactyly1 test
  • Sickle cell-hemoglobin C disease1 test
  • Silver-Russell syndrome 11 test
  • Silver-Russell syndrome due to an imprinting defect of 11p151 test
  • Spinal muscular atrophy1 test
  • Stickler syndrome type 11 test
  • Tay-Sachs disease1 test
  • Thanatophoric dysplasia type 11 test
  • Thrombophilia due to activated protein C resistance1 test
  • Thrombophilia due to thrombin defect1 test
  • Thyroid hormone resistance syndrome1 test
  • TNF receptor-associated periodic fever syndrome (TRAPS)1 test
  • Turcot syndrome2 tests
  • Type II Collagenopathies1 test
  • Ulnar-mammary syndrome1 test
  • Uniparental disomy of 71 test
  • Upshaw-Schulman syndrome1 test
  • Usher syndrome type 1B1 test
  • Usher syndrome type 1C1 test
  • Usher syndrome type 1D1 test
  • Usher syndrome type 1F1 test
  • Usher syndrome type 2A1 test
  • Usher syndrome type 2C1 test
  • Usher syndrome type 2D1 test
  • Usher syndrome type 31 test
  • Von Hippel-Lindau syndrome1 test
  • Waardenburg syndrome type 11 test
  • Waardenburg syndrome type 2A1 test
  • Waardenburg syndrome type 31 test
  • Wilms tumor 11 test
  • Wilson disease1 test
  • X-linked Alport syndrome1 test
  • X-linked mixed hearing loss with perilymphatic gusher1 test
  • Y chromosome-related disorders1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Uniparental Disomy (UPD) Testing

List of certifications/licenses

Certifications

  • CLIAHelp, Number: 99D0999793, Expiration date: 2018-04-30
  • CAP, Number: 2998501, Expiration date: 2017-06-10

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.